A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788329



Internal ID18813937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45316497..45672399hg38UCSC Ensembl
Innerchr10:45811945..46167847hg19UCSC Ensembl
Innerchr10:45131951..45487853hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38355903
hg19355903
hg18355903
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891797
Supporting Variants
Samples
Known GenesALOX5, MARCH8, ZFAND4
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=53
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788329
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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